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Reply to the letter from Gazulla et al.

Authors :
Corcia, Philippe
Lunetta, Christian
Couratier, Philippe
Vourc'h, Patrick
Gromicho, Marta
Desnuelle, Claude
Soriani, Marie‐Hélène
Pinto, Susana
de Carvalho, Mamede
Source :
European Journal of Neurology; Jan2022, Vol. 29 Issue 1, pe3-e4, 2p
Publication Year :
2022

Abstract

However, we completely agree with Dr Gazulla et al.'s assumption that PLS, like ALS, is not a pure motor neurone disease but rather a multisystem neurodegenerative disease defined by a predominant motor system injury. Moreover, Bede's team has demonstrated the existence of cerebellar atrophy in sporadic ALS and in ALS linked to I C9orf72 i abnormal G4C2 expansion [5,6]. We read with great interest the letter of Drs Gazulla and collaborators, who suggested that the continuum between primary lateral sclerosis (PLS) and amyotrophic lateral sclerosis (ALS) is not straightforward [1]. [Extracted from the article]

Details

Language :
English
ISSN :
13515101
Volume :
29
Issue :
1
Database :
Complementary Index
Journal :
European Journal of Neurology
Publication Type :
Academic Journal
Accession number :
154044631
Full Text :
https://doi.org/10.1111/ene.15134